The Journal of Organic Chemistry,
Год журнала:
2024,
Номер
unknown
Опубликована: Ноя. 22, 2024
A
novel
Cu/Pd-catalyzed
domino
radical
cyclization
and
C-H
carbonylation
of
α-bromocarbonyls
has
been
developed,
which
enables
the
rapid
incorporation
CO
unit
into
polycyclic
quinolin-2(1
Organic & Biomolecular Chemistry,
Год журнала:
2024,
Номер
unknown
Опубликована: Янв. 1, 2024
β-Enaminone
transformation
strategies
are
widely
employed
in
the
synthesis
of
numerous
biologically
active
drugs
and
natural
products,
highlighting
their
significance
medicinal
chemistry.
Chinese Journal of Chemistry,
Год журнала:
2023,
Номер
41(24), С. 3751 - 3771
Опубликована: Сен. 4, 2023
Comprehensive
Summary
Fused
polycyclic
N
‐heterocycles
are
very
important
scaffolds
in
biomedicinal
chemistry
and
materials
science.
Intramolecular
alkyne
hydroamination
is
a
powerful
method
for
the
construction
of
‐heterocycles.
In
last
two
decades,
copper‐catalyzed
domino
reactions
based
on
intramolecular
has
emerged
as
robust
strategy
assembling
various
fused
Great
progress
been
achieved
this
area.
This
short
review
covers
advances
made
synthesis
from
2008
to
2023,
will
hopefully
serve
an
inspiration
towards
exploration
new
versions
transformation.
The
transformations
introduced
discussed
five
aspects
according
different
key
processes
involved
these
reactions.
Green Synthesis and Catalysis,
Год журнала:
2023,
Номер
unknown
Опубликована: Окт. 1, 2023
The
synthesis
of
4-halo-functionalized
pyrazoles
by
electrochemical
cascade
reactions
between
N,N-dimethyl
enaminones
and
proper
hydrazine
reagents
in
the
presence
a
halogen
source
is
realized
at
room
temperature.
work
provides
tunable
efficient
accesses
to
4-chloro-
4-bromopyrazoles
aqueous
THF
(tetrahydrofuran)
without
using
any
transition
metal
reagent.
Applied Organometallic Chemistry,
Год журнала:
2024,
Номер
38(9)
Опубликована: Июль 5, 2024
A
novel
Rh‐catalyzed
three‐component
synthesis
of
N
‐(
o
‐alkylaryl)
pyrazoles
via
cascade
pyrazole
annulation
and
aryl
C‐H
conjugate
addition
to
alkenes
has
been
developed
with
enaminones,
hydrazines,
functionalized
as
starting
materials.
The
raw
materials
used
in
this
reaction
are
simple,
cheap,
readily
available,
the
reactions
feature
excellent
step
economy
by
furnishing
products
formation
a
ring
key
activation
one‐step
operation.
Moreover,
proceeds
smoothly
under
air
atmosphere,
making
it
easy
operate.
The Journal of Organic Chemistry,
Год журнала:
2025,
Номер
unknown
Опубликована: Май 16, 2025
In
this
study,
we
reported
the
utilization
of
vinylsulfonium
salt
as
a
highly
efficient
dipolarophile,
leveraging
facile
leaving
ability
its
sulfide
moiety,
to
engage
in
[3
+
2]
cycloaddition
with
N-amino(iso)quinolinium
salts.
This
approach
facilitates
construction
various
C1/C2-unsubstituted
pyrazolo(iso)quinoline
skeletons.
The
transformation
is
conducted
under
catalyst-
and
external
oxidant-free
conditions.
Furthermore,
extended
gram-scale
reaction
demonstrates
practical
applicability
developed
protocol.
The Chemical Record,
Год журнала:
2024,
Номер
24(7)
Опубликована: Июль 1, 2024
Recently,
transition
metal-catalyzed
ortho-C-H
bond
activation/annulations
involving
two
internal
alkyne
molecules
have
been
extensively
used
to
synthesize
highly
substituted
polycyclic
aromatic
scaffolds.
Such
reactions
emerged
as
a
powerful
atom
and
step-economical
strategy
for
the
assembly
of
multifunctional
bioactive
molecules.
In
this
context,
we
focused
on
recent
achievements
dual
C-H
activation/annulations,
well
functionalization
diaryl/alkyl
alkynes.
Organic & Biomolecular Chemistry,
Год журнала:
2023,
Номер
21(37), С. 7611 - 7615
Опубликована: Янв. 1, 2023
DBU-mediated
[3
+
2]
cycloaddition
reaction
for
the
synthesis
of
pyrazoles.
It
is
noteworthy
that
this
constructed
two
new
C–N
bonds
and
a
C–C
bond
at
same
time,
providing
door
construction
functionalization
pyrazole
scaffolds.
The Journal of Organic Chemistry,
Год журнала:
2023,
Номер
88(13), С. 9026 - 9036
Опубликована: Июнь 12, 2023
A
concise
and
highly
efficient
synthesis
method
of
direct
esterification
aldehydes
via
Pd-catalyzed
C–H
bond
activation
aldehyde
group
has
been
developed.
The
strategy
avoids
the
preoxidation
step
or
use
condensing
agents
in
ester
synthesis,
which
is
not
only
applicable
to
various
alcohols
but
also
suitable
for
phenolics
are
usually
difficult
be
esterified.
methodology
significant
advantages
broad
substrate
scope,
mild
reaction
conditions,
nonrequirement
additional
oxidants.